Anti-DGKE Antibody

$99.00$319.00

Reactivity: Human,Rat
Applications: ELISA,WB,IHC
Conjugation: Various
Supplier: CUSABIO BIOTECH CO.

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Rabbit Anti-DGKE Antibody (CSB-PA006835ESR1HU)

Supplier: CUSABIO BIOTECH CO.

Alternative names:

DAG kinase epsilon Antibody,Diglyceride kinase epsilon Antibody,DGK-epsilon Antibody,DGKE Antibody,DAGK5 Antibody

More alternative names for the antibody
DAG kinase epsilon antibody|DAGK 5 antibody|DAGK 6 antibody|DAGK5 antibody|DAGK6 antibody|DGK antibody|DGK epsilon antibody|DGK-epsilon antibody|DGKE antibody|DGKE_HUMAN antibody|Diacylglycerol kinase epsilon 64kDa antibody|Diacylglycerol kinase epsilon antibody|Diglyceride kinase epsilon antibody
Anti-DGKE antibody [MM09826Q13] (ab211749)
Close sc-100372|sc-18303|sc-98729|sc-18302|

Recommended applications: ELISA, WB, IHC

Recommended dilution: Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Recommended protocols: check protocols

Name

Anti-DGKE Antibody

Catalogue No.

CSB-PA006835ESR1HU

Reactivity

Human, Rat

Immunogen

Recombinant human Diacylglycerol kinase epsilon protein (40-260AA)

Host

Rabbit

Applications

ELISA, WB, IHC

Recommended dilution

Recommended dilution:WB:1:500-2000,IHC:1:20-1:200

Clonality

Polyclonal

Conjugation

unconjugated

Isotype

IgG

Molecular weight

63 kDa

Purification

Antigen Affinity Purified

Storage

Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.

Database links

Entrez Gene:8526( Human), Entrez Gene:56077( Mouse), Omim:601440( Human), SwissProt:P52429( Human), SwissProt:Q9R1C6( Mouse), Unigene:239514( Human), Unigene:153695( Mouse)

Protein function

Highly selective for arachidonate-containing species of diacylglycerol (DAG). May terminate signals transmitted through arachidonoyl-DAG or may contribute to the synthesis of phospholipids with defined fatty acid composition.

Protein tissue specificity

Expressed predominantly in testis. Expressed in endothelium, platelets and podocytes (at protein level). .

Involvement in disease

Nephrotic syndrome 7 (NPHS7) [MIM:615008]: A form of nephrotic syndrome, a renal disease clinically characterized by severe proteinuria, resulting in complications such as hypoalbuminemia, hyperlipidemia and edema. NPHS7 is an autosomal recessive form characterized by onset of proteinuria usually in the first decade of life. The disorder is progressive, and some patients develop end-stage renal disease within several years. Renal biopsy typically shows membranoproliferative glomerulonephritis. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Hemolytic uremic syndrome atypical 7 (AHUS7) [MIM:615008]: An atypical form of hemolytic uremic syndrome characterized by acute onset in the first year of life of microangiopathic hemolytic anemia, thrombocytopenia, and renal failure. After the acute episode, most patients develop chronic renal insufficiency. Unlike other genetic forms of aHUS, AHUS7 is not related to abnormal activation of the complement system. . Note=Disease susceptibility is associated with variations affecting the gene represented in this entry.

Protein sequence and domain

Belongs to the eukaryotic diacylglycerol kinase family.

Protein cellular localization

Membrane ; Multi-pass membrane protein . Membrane . Cytoplasm .

Research area

All research areas>Kinases and Phosphatases>DGK
(View all antibody categories related to Kinases and Phosphatases)

Note

AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.

Supplier

CUSABIO BIOTECH CO.

Product type

Primary antibody

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